Phenotypes for disease #04569 (CMT2U (Charcot-Marie-Tooth disease, axonal, type 2U (CMT-2U)), OMIM:616280)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000068576 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00079369
0000068577 see paper; ... - - Familial, autosomal dominant - - - - - Johan den Dunnen 00079368
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